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通过单分子系链粒子运动探测DNA中无标记的局部弯曲

Probing a label-free local bend in DNA by single molecule tethered particle motion.

作者信息

Brunet Annaël, Chevalier Sébastien, Destainville Nicolas, Manghi Manoel, Rousseau Philippe, Salhi Maya, Salomé Laurence, Tardin Catherine

机构信息

CNRS; LPT (Laboratoire de Physique Théorique); UMR UPS-CNRS 5152; 118 route de Narbonne, F-31062 Toulouse, France Université de Toulouse; UPS; LPT; F-31062 Toulouse, France CNRS; IPBS (Institut de Pharmacologie et de Biologie Structurale); UMR UPS-CNRS 5089; 205 route de Narbonne, F-31077 Toulouse, France Université de Toulouse; UPS; IPBS; F-31077 Toulouse, France.

CNRS; IPBS (Institut de Pharmacologie et de Biologie Structurale); UMR UPS-CNRS 5089; 205 route de Narbonne, F-31077 Toulouse, France Université de Toulouse; UPS; IPBS; F-31077 Toulouse, France.

出版信息

Nucleic Acids Res. 2015 Jun 23;43(11):e72. doi: 10.1093/nar/gkv201. Epub 2015 Mar 12.

Abstract

Being capable of characterizing DNA local bending is essential to understand thoroughly many biological processes because they involve a local bending of the double helix axis, either intrinsic to the sequence or induced by the binding of proteins. Developing a method to measure DNA bend angles that does not perturb the conformation of the DNA itself or the DNA-protein complex is a challenging task. Here, we propose a joint theory-experiment high-throughput approach to rigorously measure such bend angles using the Tethered Particle Motion (TPM) technique. By carefully modeling the TPM geometry, we propose a simple formula based on a kinked Worm-Like Chain model to extract the bend angle from TPM measurements. Using constructs made of 575 base-pair DNAs with in-phase assemblies of one to seven 6A-tracts, we find that the sequence CA6CGG induces a bend angle of 19° ± 4°. Our method is successfully compared to more theoretically complex or experimentally invasive ones such as cyclization, NMR, FRET or AFM. We further apply our procedure to TPM measurements from the literature and demonstrate that the angles of bends induced by proteins, such as Integration Host Factor (IHF) can be reliably evaluated as well.

摘要

能够表征DNA局部弯曲对于深入理解许多生物过程至关重要,因为这些过程涉及双螺旋轴的局部弯曲,这种弯曲要么是序列固有的,要么是由蛋白质结合诱导的。开发一种不干扰DNA本身或DNA-蛋白质复合物构象的测量DNA弯曲角度的方法是一项具有挑战性的任务。在此,我们提出一种理论与实验相结合的高通量方法,使用 tethered Particle Motion(TPM)技术严格测量此类弯曲角度。通过仔细对TPM几何结构进行建模,我们基于扭结的蠕虫状链模型提出一个简单公式,用于从TPM测量中提取弯曲角度。使用由575个碱基对的DNA制成的构建体,其中包含一到七个6A序列的同相组装,我们发现序列CA6CGG诱导的弯曲角度为19°±4°。我们的方法成功地与理论上更复杂或实验上更具侵入性的方法(如环化、核磁共振、荧光共振能量转移或原子力显微镜)进行了比较。我们进一步将我们的程序应用于文献中的TPM测量,并证明蛋白质(如整合宿主因子(IHF))诱导的弯曲角度也可以可靠地评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9873/4477641/040adefae07c/gkv201fig1.jpg

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